FDA Device Intelligence
HomeYOUNG DENTAL MANUFACTURING I, LLC › Denticator

Denticator

YOUNG DENTAL MANUFACTURING I, LLC · Model 530700 · UDI-DI 00302735307004

EHK Prescription
8
510(k) clearances
3
Adverse events
1
Recalls
121
Facilities

Description

Denticator Prophy Cup, Regular Firm, Regular Size White 4-Web Cup, Metal Latch Type, Bulk Buy

Recalls

DateFirmReason
2023-07-20Cosmedent, Inc.Reports were received the elastomer cup material is crumbling.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.